{
    "disease_id": "DOID:0110868",
    "recommended_name": {
        "id": "DOID:0110868",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110868",
        "name": "congenital stationary night blindness 1D",
        "description": "A congenital stationary night blindness characterized by a Riggs type of electroretinogram (proportionally reduced a- and b-waves) that has_material_basis_in homozygous or compound heterozygous mutation in the SLC24A1 gene on chromosome 15q22."
    },
    "synonyms": [
        {
            "id": "DOID:0110868",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110868",
            "name": "CSNB1D",
            "description": ""
        },
        {
            "id": "DOID:0110868",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110868",
            "name": "congenital stationary night blindness 1D autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0013450",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013450",
            "name": "congenital stationary night blindness 1D",
            "description": "Any congenital stationary night blindness in which the cause of the disease is a mutation in the SLC24A1 gene."
        },
        {
            "id": "MONDO:0013450",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013450",
            "name": "CSNB1D",
            "description": ""
        },
        {
            "id": "MONDO:0013450",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013450",
            "name": "SLC24A1 congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0013450",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013450",
            "name": "congenital stationary night blindness 1D",
            "description": ""
        },
        {
            "id": "MONDO:0013450",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013450",
            "name": "congenital stationary night blindness caused by mutation in SLC24A1",
            "description": ""
        },
        {
            "id": "MONDO:0013450",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013450",
            "name": "congenital stationary night blindness type 1D",
            "description": ""
        },
        {
            "id": "MONDO:0013450",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013450",
            "name": "night blindness, congenital stationary (complete), 1D, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0013450",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013450",
            "name": "night blindness, congenital stationary, type 1D",
            "description": ""
        },
        {
            "id": "MIM:613830",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613830",
            "name": "Night blindness, congenital stationary, 1D",
            "description": "Night blindness, congenital stationary, 1D"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110868"
    ],
    "unlinked_id_list": []
}